Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID02548546

Estimation of Biomechanical Aortic Wall Properties in Healthy and Aneurysmal Aortas Using Novel Imaging Techniques

Led by Mayo Clinic · Updated on 2025-09-11

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to assess the practicality of two new imaging techniques for measuring the biomechanical properties of the aorta in patients with abdominal aortic aneurysm (AAA) and healthy individuals. The study involves comparing groups with no surgery, open surgery, and endovascular aneurysm repair (EVAR) to understand relationships between aortic wall properties and clinical outcomes such as aneurysm growth and rupture risk. Patients who meet surgery indications including symptomatic AAA, large size, or rapid growth will undergo standard preoperative assessments modified to include ECG-gated magnetic resonance angiogram (MRA) and 2-dimensional speckle-tracking ultrasound (ECHO) of the abdominal aorta. These imaging methods will be used across the three patient groups: surveillance without surgery, open surgery, and EVAR. Patients will be followed for one year to monitor changes. Participants will receive imaging assessments including ECHO and ECG-gated MRA at baseline and during follow-up. Researchers will analyze changes in ECHO imaging as the primary outcome and changes in ECG-gated MRA as a secondary outcome. Patients with AAA will be monitored for aneurysm progression and related clinical events. The study does not use random assignment or masking, and participation will involve standard preoperative and follow-up imaging over one year.

CONDITIONS

Brief Title

Estimation of Biomechanical Aortic Wall Properties in Healthy and Aneurysmal Aortas Using Novel Imaging Techniques

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years of age who can provide informed consent
  • Patients with symptomatic or asymptomatic abdominal aortic aneurysm defined as aortic diameter at least 1.5 times normal
  • Patients with non-aneurysmal aortas requiring aortic contrast imaging or echocardiography for preoperative planning or other reasons
Not Eligible

You will not qualify if you...

  • Patients allergic to intravenous contrast or with severe kidney dysfunction
  • Patients not requiring contrast imaging or echocardiogram as part of their care plan
  • Terminally ill patients or those with life expectancy 6 months or less
  • Patients unable to tolerate magnetic resonance imaging

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Pre-operative period as per routine care

Participants undergo imaging studies, including ECHO and ECG-gated MRA, to assess aortic wall properties before any intervention.

1 to 2 visits depending on group assignment

Surveillance

Duration - Up to 1 year

Participants with no surgery are monitored using ECHO and ECG-gated MRA imaging to observe aortic aneurysm status.

Periodic imaging visits during the year

Surgery

Duration - Duration of surgical intervention and immediate care

Participants undergo open surgery or EVAR to repair the aortic aneurysm with associated imaging assessments.

1 surgical visit plus standard post-operative imaging visits

Long-term Monitoring

Duration - Up to 1 year after intervention or surveillance

Participants are followed for up to 1 year with imaging assessments to monitor aortic wall properties and clinical outcomes after surgery or surveillance.

Multiple imaging visits during follow-up

Trial Site Locations

Total: 1 location

1

Mayo Clinic Florida

Jacksonville, Florida, United States, 32224

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Research Team

H

Houssam Farres, MD

M

Mauricia Buchanan, RN

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

3

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Frequently Asked Questions

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